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Triethylamine → 3-(2-Chloro-6-trifluoromethyl-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane

HRID 75450
ノート
印刷プレビュー

反応式

HRID 75450 の反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1.Cl.[CH:14]12[O:21][CH:18]([CH2:19][CH2:20]1)[CH2:17][NH:16][CH2:15]2.C(N(CC)CC)C>C(OCC)C.C(O)C>[Cl:1][C:2]1[N:7]=[C:6]([N:16]2[CH2:15][CH:14]3[O:21][CH:18]([CH2:19][CH2:20]3)[CH2:17]2)[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8471Triethylamine2 回HCID 3342032,4-Dichloro-6-(trifluoromethyl)pyrimidineHCID 219835368-Oxa-3-aza-bicyclo(3.2.1)octane hydrochloride2 回

生成物 1

HCID 866659013-(2-Chloro-6-trifluoromethyl-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane収率 120.2%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 3283
Diethyl Ether
溶媒

実験手順

A solution of crude 2,4-dichloro-6-(trifluoromethyl)pyrimidine (62, 6.7 mmol) in diethyl ether (10 mL) was diluted with ethanol (25 mL) and cooled in an ice-water bath. 8-Oxa-3-azabicyclo[3.2.1]octane hydrochloride (2, 3.4 mmol) was added, followed by triethylamine (2 mL). Two additional portions of 8-oxa-3-azabicyclo[3.2.1]octane hydrochloride (2, 100 mg each) were added, the mixture was slowly warmed to room temperature and stirred overnight. Additional triethylamine (4 mL) was added to the mixture, which was then concentrated to dryness under reduced pressure. The residue was purified via flash silica gel chromatography (40% ethyl acetate/hexanes) to provide the title compound as a light colored solid (1.2 g, 61%). MS (ES+): 294.2 (M+H)+.

後処理

  1. temperaturecooled in an ice-water bath
  2. concentrationwas then concentrated to dryness under reduced pressure
  3. customThe residue was purified via flash silica gel chromatography (40% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-388ffe1582cc46c48dd18fce67d6cdc3
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08835429B2

反応ノート

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